GapMind for catabolism of small carbon sources

 

Alignments for a candidate for x5p-reductase in Sinorhizobium meliloti 1021

Align Lmo2663 protein (characterized, see rationale)
to candidate SMc01214 SMc01214 zinc-containing alcohol dehydrogenase

Query= uniprot:Q8Y414
         (343 letters)



>FitnessBrowser__Smeli:SMc01214
          Length = 347

 Score =  187 bits (475), Expect = 3e-52
 Identities = 123/344 (35%), Positives = 180/344 (52%), Gaps = 10/344 (2%)

Query: 1   MKAVVKTNPGYDQMELKDVEEPQVYGDKVKIKVAFTGICGSDIHTFKGEYKNPTTPVTLG 60
           MKAV   + G   + +++V  P+   D + +KV   GICG+D H   GE+ + T PVTLG
Sbjct: 1   MKAVRLESVG--NISVRNVGIPEPGPDDLLVKVEACGICGTDRHLLHGEFPS-TPPVTLG 57

Query: 61  HEFSGVVVEVGPDVTSIKVGDRVTSETTFETCGECIYCKEHDYNLCSNRRGIGTQANGSF 120
           HEF G+VVE G  V  I  G R+T +    +CG C  C+    NLC N R IG   +G F
Sbjct: 58  HEFCGIVVEAGSAVRDIAPGARITGDPNI-SCGRCPQCQAGRVNLCRNLRAIGIHRDGGF 116

Query: 121 AEFVLSREESCHVLDERISLEAAALTEPLACCVHSALEKTTIRPDDTVLVFGPGPIGLLL 180
           AE+VL   +    +   +     A  EPLACC+H  ++ + I+   TV + G G IGLL 
Sbjct: 117 AEYVLVPRKQAFEIPLTLDPVHGAFCEPLACCLH-GVDLSGIKAGSTVAILGGGVIGLLT 175

Query: 181 AQVVKAQGATVIMAGITKDSDRLRLAKELGMDRIVDTLKEDLAEVVLGMTG--GYGAERV 238
            Q+ +  GAT ++   T+ + + RLA+E+G    VD    D+ E + G  G    G + V
Sbjct: 176 VQLARLAGATTVILS-TRQATKRRLAEEVGATATVDPSAGDVVEAIAGPVGLVPGGVDVV 234

Query: 239 FDCSGAVPAVNQGLPLTKKKGDFVQVGLFAE-KKNAIDEESIIQREIAYIGSRSQKPSSW 297
            +C+G    V Q   L K  G  V +G+  + +K  I+   I+ RE+  +GS    P   
Sbjct: 235 IECAGVAETVKQSTRLAKAGGTVVILGVLPQGEKVEIEPFDILFRELRVLGS-FINPFVH 293

Query: 298 ILALDLLANGKIDTDKMITKVYGLDDWREAFEAVMAGNEIKVLV 341
             A DL+A G I+ D+MI++   LD+  +      A  E+KVLV
Sbjct: 294 RRAADLVATGAIEIDRMISRRISLDEAPDVISNPAAAGEVKVLV 337


Lambda     K      H
   0.317    0.135    0.392 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 324
Number of extensions: 22
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 343
Length of database: 347
Length adjustment: 29
Effective length of query: 314
Effective length of database: 318
Effective search space:    99852
Effective search space used:    99852
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory